We are seeking an experienced IT Business Partner to serve as the strategic technology liaison for our Medical Affairs, Regulatory Affairs, Clinical Development, and Drug Safety (Pharmacovigilance) functions. This individual will partner closely with business leaders to shape technology roadmaps, drive digital transformation initiatives, and optimize enterprise platforms that support the end-to-end pharmaceutical product lifecycle.
About the Role
The successful candidate will possess deep knowledge of the pharmaceutical industry and hands-on experience with Veeva platform solutions and Pharmacovigilance/Safety systems, enabling them to bridge business objectives with technology capabilities while ensuring compliance with global regulatory requirements.
Responsibilities
Strategic Business Partnership
Act as the trusted technology advisor to Medical, Regulatory, Clinical Operations, and Pharmacovigilance stakeholders.
Develop strong relationships with executive and functional leaders to understand business priorities, challenges, and opportunities.
Translate business strategies into technology roadmaps and investment plans.
Lead demand management, prioritization, and governance processes across the business portfolio.
Drive the strategy, adoption, optimization, and lifecycle management of key GxP-regulated applications.
Oversee technology solutions supporting:
Clinical Development
Clinical Operations
Regulatory Affairs
Medical Affairs
Pharmacovigilance and Drug Safety
Ensure alignment between enterprise architecture, data, integration, and business objectives.
Provide leadership and strategic oversight across Veeva solutions, including:
Veeva Medical CRM
Partner with business teams to identify opportunities for process automation, standardization, and optimization.
Pharmacovigilance & Safety Systems
Support and enhance integral drug safety platforms and processes.
Collaborate with Safety, Regulatory, and Quality teams to ensure compliance with health authority requirements.




Experience with one or more of the following is highly desirable:
Oracle Argus Safety
ArisGlobal LifeSphere
Safety databases and case processing solutions
Drive initiatives related to safety reporting, signal detection, risk management, and regulatory submissions.
Lead complex cross-functional transformation programs from strategy through implementation.
Manage technology vendors, system integrators, and consulting partners.
Ensure projects are delivered on time, within budget, and meeting quality and compliance requirements.
Oversee change management, communications, training, and stakeholder adoption activities.
Compliance & Governance
Ensure solutions comply with:
GxP
FDA regulations
EMA guidelines
ICH standards
21 CFR Part 11
Data privacy requirements (GDPR and applicable regulations)
Support validation and audit activities for regulated systems.
Qualifications
Bachelor's degree in Information Technology, Computer Science, Life Sciences, Pharmacy, or related discipline.
8+ years' experience in IT Business Relationship Management, IT Business Partnering, Digital Transformation, or Enterprise Applications within the pharmaceutical or life sciences industry.
Required Skills
Strong understanding of:
Clinical Development
Regulatory Affairs
Medical Affairs
Proven experience delivering and supporting enterprise platforms in regulated environments.
Demonstrable experience with the Veeva Suite, ideally including Vault Clinical and Vault RIM.
Experience with Pharmacovigilance platforms such as Argus, LifeSphere, or Veeva Safety.
Strong knowledge of application integration, data management, and enterprise technologies.
Experience managing external vendors and technology partners.
Preferred Skills
Experience supporting global pharmaceutical or biotechnology organizations.
Understanding of R&D; digital ecosystems and clinical trial technologies.
Experience with cloud platforms and SaaS application delivery models.
Knowledge of AI, automation, and advanced analytics applications within Life Sciences.
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📌 Information Technology Business Partner (Barcelona)
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